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5-BROMOTRYPTOPHAN ETHYL ESTER

Base Information Edit
  • Chemical Name:5-BROMOTRYPTOPHAN ETHYL ESTER
  • CAS No.:133766-36-6
  • Molecular Formula:C13H15BrN2O2
  • Molecular Weight:311.17
  • Hs Code.:2933990090
  • Mol file:133766-36-6.mol
5-BROMOTRYPTOPHAN ETHYL ESTER

Synonyms:5-BROMOTRYPTOPHAN ETHYL ESTER

Suppliers and Price of 5-BROMOTRYPTOPHAN ETHYL ESTER
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • Labseeker
  • ethyl2-amino-3-(5-bromo-1H-indol-3-yl)propanoate 95
  • 25g
  • $ 2475.00
  • Labseeker
  • ethyl2-amino-3-(5-bromo-1H-indol-3-yl)propanoate 95
  • 10g
  • $ 2163.00
  • Crysdot
  • Ethyl2-amino-3-(5-bromo-1H-indol-3-yl)propanoate 95+%
  • 1g
  • $ 608.00
  • Chemenu
  • ethyl2-amino-3-(5-bromo-1H-indol-3-yl)propanoate 95%
  • 1g
  • $ 574.00
  • American Custom Chemicals Corporation
  • 5-BROMOTRYPTOPHAN ETHYL ESTER 95.00%
  • 5MG
  • $ 497.56
Total 4 raw suppliers
Chemical Property of 5-BROMOTRYPTOPHAN ETHYL ESTER Edit
Chemical Property:
  • Vapor Pressure:0mmHg at 25°C 
  • Boiling Point:448.123°C at 760 mmHg 
  • Flash Point:224.817°C 
  • PSA:68.11000 
  • Density:1.497g/cm3 
  • LogP:3.06360 
  • Storage Temp.:2-8°C 
Purity/Quality:

99% *data from raw suppliers

ethyl2-amino-3-(5-bromo-1H-indol-3-yl)propanoate 95 *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
Technology Process of 5-BROMOTRYPTOPHAN ETHYL ESTER

There total 1 articles about 5-BROMOTRYPTOPHAN ETHYL ESTER which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
(+/-)-2-amino-3-(5-bromo-1H-indol-3-yl)-propionic acid ethyl ester; With potassium chloride; water; α-chymotrypsin; In acetonitrile; for 6h; pH=7; Enzymatic reaction;
With sodium hydroxide; In water; ethyl acetate; pH=12 - 13;
Refernces Edit
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